JP2014186194A - Electrostatic charge image developing toner - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an electrostatic charge image developing toner capable of obtaining a thermal resistant storage property while having low-temperature fixability and long term stability of electrification performance.SOLUTION: An electrostatic charge image developing toner includes a toner particle having a binder resin. The binder resin includes a domain matrix structure in which a crystalline polyester resin is dispersed as a domain phase in a matrix phase by an amorphous vinyl polymer formed using at least a vinyl monomer. The amorphous vinyl polymer has a carboxy group concentration of 0.2-1.0 mmol/g. The crystalline polyester resin has an ester group concentration of 0.1-7.1 mmol/g.

Description

  The present invention relates to an electrostatic charge image developing toner used for electrophotographic image formation.

  In recent years, in order to further save energy in an electrophotographic image forming apparatus, an electrostatic image developing toner (hereinafter also simply referred to as “toner”) that is thermally fixed at a lower temperature is required. ing. Such toners are required to have further excellent low-temperature fixability and long-term stability of charging performance so that high-quality images can be formed over a long period of time.

For example, Patent Document 1 discloses a toner containing a crystalline polyester resin as a fixing aid.
However, in such a toner, the following problems occur if the compatibility between the crystalline polyester resin and the binder resin is not taken into consideration. For example, when the crystalline polyester resin and the binder resin at the time of heat fixing are highly compatible, since the plasticization of the binder resin proceeds before heat fixing, there is a problem that the heat resistant storage property is poor. . On the other hand, when the crystalline polyester resin and the binder resin are low in compatibility, there is a problem that sufficient low-temperature fixability cannot be obtained. When the toner is exposed to the toner and the chargeability of the toner is lowered, there is a problem that an image defect such as a decrease in image density and fogging occurs.

Therefore, for example, in Patent Document 2, by controlling the affinity between the binder resin and the crystalline polyester resin and the ester group concentration of the crystalline polyester resin, both low-temperature fixability and long-term stability of the charging performance are achieved. It has been proposed.
However, in Patent Document 2, although compatibility between the crystalline polyester resin and the binder resin is considered, since the binder resin is a combination of the same resin species as the polyester resin, the low-temperature fixability and the heat-resistant storage are achieved. However, there is a problem that the charging performance is inferior in long-term stability. In addition, although compatibility is controlled, there is a problem that exposure to the surface of the crystalline polyester cannot be completely suppressed because of the same resin type.

  Patent Document 3 proposes to use a combination of a copolymer formed of a styrene monomer and a (meth) acrylate monomer and a crystalline polyester resin as a binder resin. . The crystalline polyester resin surface is taken in by seeding with the same type of resin as the binder resin to achieve both low-temperature fixability and heat-resistant storage stability, but completely suppresses the surface exposure of the crystalline polyester from the binder resin. There has been a problem that compatibility has not been studied and long-term stability of charging is poor.

JP 2001-222138 A JP 2011-81355 A JP 2011-197659 A

  The present invention has been made in consideration of the above circumstances, and its purpose is to develop an electrostatic charge image that has a low temperature fixability and a long-term stability of charging performance, and can obtain heat-resistant storage stability. It is to provide a toner.

The electrostatic image developing toner of the present invention is an electrostatic image developing toner comprising toner particles containing a binder resin,
The binder resin has a domain matrix structure in which a crystalline polyester resin is dispersed as a domain phase in a matrix phase of an amorphous vinyl polymer formed using at least a vinyl monomer,
The amorphous vinyl polymer has a carboxy group concentration of 0.2 mmol / g or more and 1.0 mmol / g or less,
The crystalline polyester resin has an ester group concentration of 0.1 mmol / g or more and 7.1 mmol / g or less.

  In the toner for developing an electrostatic charge image of the present invention, the mass ratio of the amorphous vinyl polymer to the crystalline polyester resin (amorphous vinyl polymer / crystalline polyester resin) is 97/3 to 60/40. It is preferable that

  In the electrostatic image developing toner of the present invention, the crystalline polyester resin preferably has a melting point of 40 to 95 ° C.

In the electrostatic image developing toner of the present invention, the amorphous vinyl polymer includes two types of amorphous vinyl polymer A and amorphous vinyl polymer B having different carboxy group concentrations,
The toner particles are obtained by agglomerating and fusing the composite fine particles in which the amorphous vinyl polymer B is adhered to the surfaces of the fine particles of the crystalline polyester resin and the fine particles of the amorphous vinyl polymer A. It is preferable that

  In the electrostatic image developing toner of the present invention, the composite fine particles have a mass ratio of the crystalline polyester resin to the amorphous vinyl polymer B (crystalline polyester resin / amorphous vinyl polymer B). It is preferably 10/90 to 80/20.

In the electrostatic image developing toner of the present invention, the amorphous vinyl polymer B in the composite fine particles has a carboxy group concentration of 0.2 mmol / g or more and 1.0 mmol / g or less,
When the carboxy group concentration of the amorphous vinyl polymer A is A1 [mmol / g] and the carboxy group concentration of the amorphous vinyl polymer B is B1 [mmol / g], the following relational expression (1) and It is preferable to satisfy (2).
Relational expression (1): B1 <A1
Relational expression (2): A1-B1 ≦ | 0.5 |

  According to the electrostatic image developing toner of the present invention, the binder resin has a domain matrix structure, the carboxy group concentration of the amorphous vinyl polymer constituting the matrix phase, and the crystalline polyester constituting the domain phase. When the ester group concentration of the resin is in a specific range, heat-resistant storage stability can be obtained while having low-temperature fixability and long-term stability of charging performance.

  Hereinafter, the present invention will be described in detail.

〔toner〕
The toner of the present invention comprises toner particles containing at least a binder resin, and the toner particles contain other toner components such as a colorant, a magnetic powder, a release agent, and a charge control agent as desired. Can be. Further, external additives such as a fluidizing agent and a cleaning aid may be added to the toner particles.
The toner of the present invention is obtained by a wet production method produced in an aqueous medium, for example, an emulsion aggregation method.

[Binder resin]
In the toner of the present invention, the binder resin contains at least a crystalline polyester resin and an amorphous vinyl polymer. The binder resin has a domain matrix structure in which a crystalline polyester resin is dispersed as a domain phase in a matrix phase of an amorphous vinyl polymer.

Here, the domain matrix structure means a structure in which a domain phase having a closed interface (boundary between phases) exists in a continuous matrix phase. The toner of the present invention shows a state in which a crystalline polyester resin is introduced incompatible with an amorphous vinyl polymer.
This structure can be observed by measuring a cross section of an osmium-dyed toner particle with a transmission electron microscope by a conventional method. In the case of cutting a section with an ultramicrotome, the thickness of the section is set to 100 nm.

(Amorphous vinyl polymer)
The amorphous vinyl polymer constituting the matrix phase is constituted as a main component in the binder resin, and is formed using at least a vinyl monomer.

  Specific examples of the amorphous vinyl polymer include acrylic resins and styrene acrylic copolymer resins.

Examples of the vinyl monomer that forms the amorphous vinyl polymer include the following. As a vinyl-type monomer, it can be used individually by 1 type or in combination of 2 or more types.
(1) Styrene monomer Styrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, α-methylstyrene, p-phenylstyrene, p-ethylstyrene, 2,4-dimethylstyrene, p-tert -Butyl styrene, pn-hexyl styrene, pn-octyl styrene, pn-nonyl styrene, pn-decyl styrene, pn-dodecyl styrene, and derivatives thereof.
(2) (meth) acrylic acid ester monomer (meth) methyl acrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, isopropyl (meth) acrylate, isobutyl (meth) acrylate, T-butyl (meth) acrylate, n-octyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, stearyl (meth) acrylate, lauryl (meth) acrylate, phenyl (meth) acrylate, (meth ) Diethylaminoethyl acrylate, dimethylaminoethyl (meth) acrylate, and derivatives thereof.
(3) Vinyl esters Vinyl propionate, vinyl acetate, vinyl benzoate and the like.
(4) Vinyl ethers Vinyl methyl ether, vinyl ethyl ether and the like.
(5) Vinyl ketones Vinyl methyl ketone, vinyl ethyl ketone, vinyl hexyl ketone and the like.
(6) N-vinyl compounds N-vinylcarbazole, N-vinylindole, N-vinylpyrrolidone and the like.
(7) Others Vinyl compounds such as vinyl naphthalene and vinyl pyridine, acrylic acid or methacrylic acid derivatives such as acrylonitrile, methacrylonitrile and acrylamide.

Moreover, as a vinyl-type monomer, it is preferable to use the monomer which has ionic dissociation groups, such as a carboxy group, a sulfonic acid group, a phosphoric acid group, for example. Specifically, there are the following.
Examples of the monomer having a carboxy group include acrylic acid, methacrylic acid, maleic acid, itaconic acid, cinnamic acid, fumaric acid, maleic acid monoalkyl ester, itaconic acid monoalkyl ester, and the like. Examples of the monomer having a sulfonic acid group include styrene sulfonic acid, allyl sulfosuccinic acid, 2-acrylamido-2-methylpropane sulfonic acid, and the like. Furthermore, examples of the monomer having a phosphate group include acid phosphooxyethyl methacrylate.
In the present invention, it is essential to use a monomer having a carboxy group as the vinyl monomer, and the ratio of the monomer having a carboxy group in all vinyl monomers is 2-7. It is preferable that it is mass%. When the proportion of the monomer having a carboxy group is excessive, the amount of moisture adsorbed on the surface of the toner particles increases, which may cause generation of toner blisters and expansion of the difference in charge amount environment.

  Furthermore, polyfunctional vinyls can be used as the vinyl monomer, and the amorphous vinyl polymer can have a crosslinked structure. Polyfunctional vinyls include divinylbenzene, ethylene glycol dimethacrylate, ethylene glycol diacrylate, diethylene glycol dimethacrylate, diethylene glycol diacrylate, triethylene glycol dimethacrylate, triethylene glycol diacrylate, neopentyl glycol dimethacrylate, neopentyl glycol Examples include diacrylate.

  As the amorphous vinyl polymer, a styrene acrylic copolymer resin formed using a styrene monomer and a (meth) acrylic acid ester monomer is preferable.

The amorphous vinyl polymer has a carboxy group concentration of 0.2 mmol / g or more and 1.0 mmol / g or less, preferably 0.3 mmol / g or more and 0.85 mmol / g or less.
Here, the carboxy group concentration is the ratio of carboxy groups in the amorphous vinyl polymer, and indicates the degree of affinity for water. The larger the value, the higher the affinity for water.
When the carboxy group concentration of the amorphous vinyl polymer is in the above range, the amorphous vinyl polymer is more crystalline than the crystalline polyester resin in relation to the ester group concentration of the crystalline polyester resin constituting the domain phase described later. Is also highly hydrophilic. Therefore, at the time of toner production in an aqueous medium, while maintaining the incompatible relationship between the amorphous vinyl polymer constituting the matrix phase and the crystalline polyester resin constituting the domain phase, the crystalline polyester resin In a state dispersed in the inner side of the toner particles to be formed, specifically, the crystalline polyester resin is not exposed on the surface of the toner particles to be formed, or the amount thereof is extremely small even if exposed. Particles are formed in a state, and the obtained toner has long-term stability of charging performance while having sufficient low-temperature fixability and heat-resistant storage stability.
When the carboxy group concentration of the amorphous vinyl polymer is too low, the amorphous vinyl polymer does not exhibit high hydrophilicity compared to the crystalline polyester resin, and the toner is produced in an aqueous medium. In such a case, the crystalline polyester resin may be formed in a state where the crystalline polyester resin is exposed on the surface of the toner particles to be formed, and the obtained toner may not have long-term stability in charging performance. In addition, when the carboxy group concentration of the amorphous vinyl polymer is excessive, the carboxy group concentration of the surrounding resin becomes excessive at the time of toner production, and the amount of moisture adsorbed on the surface of the toner particles is increased. There is a possibility that generation of blisters or expansion of the difference in charge amount environment may occur.

In the present invention, the carboxy group concentration is a value calculated by the following formula (1).
Formula (1): Carboxy group concentration = [total number of moles of carboxy groups / (molecular weight of vinyl-based monomer forming amorphous vinyl polymer × mol fraction)] × 1000
The carboxy group concentration of the amorphous vinyl polymer can be controlled by the introduction ratio of the monomer having a carboxy group.
When two or more kinds of amorphous vinyl polymers having different carboxy group concentrations are used as the amorphous vinyl polymer, the carboxy group concentration is the same as the carboxy group concentration of each amorphous vinyl polymer. The sum of values multiplied by the content ratio (mass ratio).

The amorphous vinyl polymer preferably has a glass transition point (Tg) of 25 to 60 ° C, more preferably 40 to 55 ° C.
When the glass transition point of the amorphous vinyl polymer is in the above range, sufficient low-temperature fixability and heat-resistant storage stability can be reliably achieved.
When the glass transition point of the amorphous vinyl polymer is too small, the heat resistance (thermal strength) of the toner is lowered, and there is a possibility that sufficient heat storage stability and hot offset resistance may not be obtained. . Also, if the glass transition point of the amorphous vinyl polymer is excessive, sufficient low-temperature fixability may not be obtained.

In the present invention, the glass transition point (Tg) of the amorphous vinyl polymer is a value measured using “Diamond DSC” (manufactured by PerkinElmer).
As a measurement procedure, 3.0 mg of a measurement sample (amorphous vinyl polymer) is sealed in an aluminum pan and set in a holder. The reference used an empty aluminum pan. The measurement conditions were a measurement temperature of 0 ° C. to 200 ° C., a temperature increase rate of 10 ° C./min, a temperature decrease rate of 10 ° C./min, and heat-cool-heat temperature control. Perform analysis based on the data in Heat, draw a baseline extension before the rise of the first endothermic peak, and a tangent line indicating the maximum slope between the rise of the first peak and the peak apex, Let the intersection be the glass transition point.

  The amorphous vinyl polymer preferably has a molecular weight measured by gel permeation chromatography (GPC) of 10,000 to 40,000 in terms of weight average molecular weight (Mw).

In the present invention, the molecular weight of the amorphous vinyl polymer by gel permeation chromatography (GPC) is a value measured as follows.
Specifically, using an apparatus “HLC-8120GPC” (manufactured by Tosoh Corporation) and a column “TSKguardcolumn + TSKgelSuperHZ-M3 series” (manufactured by Tosoh Corporation), while maintaining the column temperature at 40 ° C., tetrahydrofuran (THF) was used as a carrier solvent. Flow at a flow rate of 0.2 ml / min, and dissolve the measurement sample (amorphous vinyl polymer) in tetrahydrofuran to a concentration of 1 mg / ml under dissolution conditions in which treatment is performed at room temperature using an ultrasonic disperser for 5 minutes. Next, a sample solution is obtained by processing with a membrane filter having a pore size of 0.2 μm, and 10 μL of this sample solution is injected into the apparatus together with the above carrier solvent, and is detected using a refractive index detector (RI detector) and measured. The molecular weight distribution of the sample was measured using monodisperse polystyrene standard particles Calculated using a calibration curve. Ten polystyrenes were used for calibration curve measurement.

(Crystalline polyester resin)
The crystalline polyester resin constituting the domain phase is a known polyester resin obtained by a polycondensation reaction of a divalent or higher carboxylic acid (polyvalent carboxylic acid) and a divalent or higher alcohol (polyhydric alcohol). In differential scanning calorimetry (DSC), it refers to a resin having a clear endothermic peak rather than a stepwise endothermic change. The clear endothermic peak specifically means a peak in which the half-value width of the endothermic peak is within 15 ° C. when measured at a rate of temperature increase of 10 ° C./min in differential scanning calorimetry (DSC). To do.

The polyvalent carboxylic acid is a compound containing two or more carboxy groups in one molecule.
Specifically, for example, saturated aliphatic dicarboxylic acids such as oxalic acid, malonic acid, succinic acid, adipic acid, sebacic acid, azelaic acid and n-dodecyl succinic acid; alicyclic dicarboxylic acids such as cyclohexanedicarboxylic acid; phthalates Aromatic dicarboxylic acids such as acid, isophthalic acid and terephthalic acid; trivalent or higher polyvalent carboxylic acids such as trimellitic acid and pyromellitic acid; and anhydrides of these carboxylic acid compounds or alkyl esters having 1 to 3 carbon atoms Etc.
These may be used individually by 1 type and may be used in combination of 2 or more type.

A polyhydric alcohol is a compound containing two or more hydroxyl groups in one molecule.
Specifically, for example, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,7-heptanediol Aliphatic diols such as 1,8-octanediol, neopentyl glycol and 1,4-butenediol; trihydric or higher polyhydric alcohols such as glycerin, pentaerythritol, trimethylolpropane and sorbitol.
These may be used individually by 1 type and may be used in combination of 2 or more type.

The crystalline polyester resin has an ester group concentration of 0.1 mmol / g or more and 7.1 mmol / g or less, preferably 3.0 mmol / g or more and 7.0 mmol / g or less.
Here, the ester group concentration is the ratio of ester groups (ester bonds) in the crystalline polyester resin, and indicates the degree of affinity for water. The larger the value, the higher the affinity for water.
When the ester group concentration of the crystalline polyester resin is in the above range, the crystalline polyester resin is more hydrophilic than the amorphous vinyl polymer in relation to the carboxy group concentration of the amorphous vinyl polymer constituting the matrix phase. The property is low. Therefore, at the time of toner production in an aqueous medium, while maintaining the incompatible relationship between the amorphous vinyl polymer constituting the matrix phase and the crystalline polyester resin constituting the domain phase, the crystalline polyester resin In a state dispersed in the inner side of the toner particles to be formed, specifically, the crystalline polyester resin is not exposed on the surface of the toner particles to be formed, or the amount thereof is extremely small even if exposed. Particles are formed in a state, and the obtained toner has long-term stability of charging performance while having sufficient low-temperature fixability and heat-resistant storage stability.
In the case where the ester group concentration of the crystalline polyester resin is excessively low, good dispersibility of the crystalline polyester resin cannot be obtained at the time of toner production in an aqueous medium, and the crystalline polyester resin aggregates. In addition, when the ester group concentration of the crystalline polyester resin is excessive, the crystalline polyester resin does not exhibit high hydrophobicity as compared with the amorphous vinyl polymer, and the toner is produced in an aqueous medium. In such a case, the crystalline polyester resin may be formed in a state where the crystalline polyester resin is exposed on the surface of the toner particles to be formed, and the obtained toner may not have long-term stability in charging performance.

In the present invention, the ester group concentration is a value calculated by the following formula (2).
Formula (2): Ester group concentration = [Average number of moles of moieties capable of forming ester groups in polyvalent carboxylic acid and polyhydric alcohol forming crystalline polyester resin / ((of polyvalent carboxylic acid and polyhydric alcohol Total molecular weight)-(molecular weight of water separated by dehydration polycondensation × number of moles of ester group))] × 1000
The ester group concentration of the crystalline polyester resin can be controlled by the type of monomer.

An example of calculating the ester group concentration of the crystalline polyester resin is shown below.
The crystalline polyester resin obtained by the polyvalent carboxylic acid represented by the following formula (a) and the polyhydric alcohol represented by the following formula (b) is represented by the following formula (c).
Formula ^{(a): HOOC-R 1} -COOH
Formula (b): HO—R ² —OH
Formula (c): - (- OCO -R 1 -COO-R 2 -) n -
“Average number of moles of the portion that can be an ester group contained in the polyvalent carboxylic acid and polyhydric alcohol forming the crystalline polyester resin” means the number of moles of the carboxy group of the polyvalent carboxylic acid forming the crystalline polyester resin And the average number of moles of hydroxyl group of the polyhydric alcohol, specifically, the number of moles of carboxy group of the polycarboxylic acid of the formula (a) “2” and the hydroxyl number of the polyhydric alcohol of the formula (b) The average is “2” with the number of moles of the group “2”.
When the molecular weight of the polyvalent carboxylic acid of the formula (a) is m1, the molecular weight of the polyhydric alcohol of the formula (b) is m2, and the molecular weight of the crystalline polyester resin of the formula (c) is m3, “(polyvalent carboxylic acid) (Molecular weight of acid and polyhydric alcohol)-(molecular weight of water separated by dehydration polycondensation × number of moles of ester group) ”is (m1 + m2) − (18 × average number of moles of ester group“ 2 ”) Therefore, the molecular weight “m3” of the crystalline polyester resin of the formula (c) is obtained.
From the above, the ester group concentration of the crystalline polyester resin represented by the formula (c) is “2 / m 3”.
In addition, when two or more polycarboxylic acids or two or more polyhydric alcohols are used in combination, the average of the carboxy group and molecular weight of each polycarboxylic acid and the average of the hydroxyl group and molecular weight of the polyhydric alcohol Become.

The crystalline polyester resin preferably has a melting point (Tm) of 40 to 95 ° C, more preferably 50 to 85 ° C.
When the melting point of the crystalline polyester resin is in the above range, sufficient low-temperature fixability and excellent hot offset resistance can be obtained.
When the melting point of the crystalline polyester resin is excessively low, the obtained toner has a low thermal strength, and there is a possibility that sufficient heat resistant storage stability and hot offset resistance cannot be obtained. Moreover, when the melting point of the crystalline polyester resin is excessively high, there is a possibility that sufficient low-temperature fixability cannot be obtained.
The melting point of the crystalline polyester resin can be controlled by the resin composition.

In the present invention, the melting point of the crystalline polyester resin is a value measured as follows.
Specifically, using a differential scanning calorimeter “Diamond DSC” (manufactured by PerkinElmer Co., Ltd.), a first temperature raising process in which the temperature is raised from 0 ° C. to 200 ° C. at an elevation rate of 10 ° C./min, a cooling rate of 10 ° C./min. Measured according to the measurement conditions (temperature rise / cooling conditions) through the cooling process of cooling from 200 ° C. to 0 ° C. and the second temperature raising process of raising the temperature from 0 ° C. to 200 ° C. at a rate of 10 ° C./min. Based on the DSC curve obtained by this measurement, the endothermic peak top temperature derived from the crystalline polyester in the first temperature raising process is taken as the melting point. As a measurement procedure, 3.0 mg of a measurement sample (crystalline polyester resin) is sealed in an aluminum pan and set in a diamond DSC sample holder. The reference used an empty aluminum pan.

The crystalline polyester resin has a molecular weight measured by gel permeation chromatography (GPC) of 5,000 to 50,000 in weight average molecular weight (Mw) and 1,500 to 25,000 in number average molecular weight (Mn). It is preferable that
The molecular weight of the crystalline polyester resin measured by gel permeation chromatography (GPC) is measured in the same manner as described above except that the crystalline polyester resin is used as a measurement sample.

The mass ratio of the amorphous vinyl polymer to the crystalline polyester resin (amorphous vinyl polymer / crystalline polyester resin) is preferably 97/3 to 60/40, more preferably 95/5 to 70. / 30.
When the mass ratio (amorphous vinyl polymer / crystalline polyester resin) is in the above range, the crystalline polyester resin constituting the domain phase is not exposed or exposed on the surface of the toner particles to be formed. Even so, an amount of the crystalline polyester resin that is extremely small and that can achieve low-temperature fixability can be introduced into the toner particles.
When the ratio of the amorphous vinyl polymer is excessive in the mass ratio (amorphous vinyl polymer / crystalline polyester resin), a sufficient amount of the crystalline polyester resin introduced into the toner particles can be obtained. Insufficient low temperature fixing may not be possible. Further, in the mass ratio (amorphous vinyl polymer / crystalline polyester resin), when the ratio of the amorphous vinyl polymer is too small, the plasticization of the amorphous vinyl polymer proceeds excessively, Sufficient heat-resistant storage stability may not be obtained, and the crystalline polyester resin constituting the domain phase may be exposed on the surface of the toner particles, so that long-term stability of charging performance can be obtained. There is a risk of not.

In the present invention, in order to measure the carboxy group concentration of the amorphous vinyl polymer, the ester group concentration and the melting point of the crystalline polyester resin, it is necessary to extract each resin contained in the toner particles. Specifically, the resin can be extracted from the toner particles as follows.
First, the toner is dissolved in methyl ethyl ketone (MEK) at room temperature (20 ° C. or more and 25 ° C. or less). Here, the amorphous vinyl polymer in the toner particles is dissolved in MEK at room temperature. Therefore, since the amorphous vinyl polymer is contained in the MEK soluble matter, the amorphous vinyl polymer can be obtained from the supernatant liquid separated by centrifugation after dissolution. On the other hand, the solid content after centrifugation is heated at 65 ° C. for 60 minutes, dissolved in tetrahydrofuran (THF), and filtered through a glass filter at 60 ° C., whereby a crystalline polyester resin is obtained from the filtrate. In addition, since crystalline polyester resin will precipitate if temperature falls during filtration by the said operation, it operates in the state kept warm.

The carboxy group concentration of the amorphous vinyl polymer can be confirmed by, for example, 12C-NMR (nuclear magnetic resonance) measurement using deuterated chloroform. Specifically, the peak of the carbon atom derived from each monomer is assigned, the monomer type and composition ratio are specified, and the carboxy group concentration is calculated.
In addition, the ester group concentration of the crystalline polyester resin should be confirmed by hydrolyzing, measuring with P-GC / MS, specifying the acid and alcohol monomer types, and calculating the ester group concentration. Can do.

In the toner described above, by using an amorphous vinyl polymer as a binder resin, and the amorphous vinyl polymer and a crystalline polyester resin having a different polarity with respect to water, these amorphous vinyl polymers and The crystalline polyester resin exhibits an incompatible relationship at the time of toner production and before heat fixing. At the time of heat fixing, the crystalline polyester resin exhibits a plastic effect on the amorphous vinyl polymer, but the glass transition point of the amorphous vinyl polymer does not decrease, so it has low temperature fixability. However, heat-resistant storage properties can be obtained.
The amorphous vinyl polymer is crystallized because the carboxy group concentration of the amorphous vinyl polymer constituting the matrix phase and the ester group concentration of the crystalline polyester resin constituting the domain phase are in a specific range. Since the affinity for water is higher than that of the crystalline polyester resin, the amorphous vinyl polymer takes in the crystalline polyester resin while confining the crystalline polyester resin in the production of the toner in the aqueous medium, so that the crystalline polyester resin is formed. Since the particles are formed in a state of being dispersed on the inner side of the toner particles to be obtained, there is no crystalline polyester resin on the surface of the obtained toner particles, or even if it is present, the amount thereof is extremely small. As a result, long-term stability of charging performance can be obtained.
On the other hand, if the amorphous vinyl polymer and the crystalline polyester resin are incompatible with each other, the both have low affinity. It may be difficult to incorporate into the coalescence.
Therefore, in the present invention, as the amorphous vinyl polymer, two types of amorphous vinyl polymer A and amorphous vinyl polymer B having different carboxy group concentrations are used, and crystalline polyester resin fine particles (hereinafter, Composite fine particles in which vinyl polymer B (hereinafter also referred to as “coating resin”) is attached to the surface of “crystalline polyester resin fine particles”) and amorphous vinyl polymer A (hereinafter “main”). The toner particles are preferably formed by agglomerating and fusing the fine particles of “resin”). As a result, the resin composition of the amorphous vinyl polymer A (main resin) and the amorphous vinyl polymer B (coating resin) adhering to the surface of the crystalline polyester resin fine particles are approximated, so that high affinity is obtained. Thus, the crystalline polyester resin is easily introduced into the amorphous vinyl polymer.

Hereinafter, a method for producing composite fine particles will be specifically described.
The composite fine particles can be produced, for example, by using a seed polymerization method. Specifically, the crystalline polyester resin fine particles are used as seeds, and a vinyl monomer is seed-polymerized on the surfaces of the crystalline polyester resin fine particles, whereby the amorphous vinyl polymer B is formed on the surfaces of the crystalline polyester resin fine particles. A composite fine particle to which is attached is obtained.

  In the toner of the present invention, the amorphous vinyl polymer A (main resin) and the amorphous vinyl polymer B (coating resin) attached to the surface of the crystalline polyester resin fine particles have the same composition, specifically Are preferably formed using the same type of vinyl monomer. As described above, the amorphous vinyl polymer A and the amorphous vinyl polymer B have the same composition, so that the affinity between the amorphous vinyl polymer A and the amorphous vinyl polymer B is increased. The crystalline polyester resin can be more efficiently introduced into the amorphous vinyl polymer during toner production.

In the composite fine particles, the mass ratio of the crystalline polyester resin as the seed resin to the amorphous vinyl polymer B (coating resin) (crystalline polyester resin / amorphous vinyl polymer B) is 10/90 to 80 / It is preferable that it is 20, More preferably, it is 50 / 50-80 / 20.
When the mass ratio (crystalline polyester resin / amorphous vinyl polymer B) is in the above range, a sufficient amount of amorphous vinyl polymer B is attached to the surface of the crystalline polyester resin fine particles. The obtained composite fine particles can form a good core-shell structure.
In the composite fine particles, the surface of the crystalline polyester resin fine particles as a seed is preferably completely covered with the amorphous vinyl polymer B, but a part of the surface of the crystalline polyester resin fine particles is amorphous. It may be coated with vinyl polymer B.

In the amorphous vinyl polymer B, the carboxy group concentration B1 is preferably 0.2 mmol / g or more and 1.0 mmol / g or less, more preferably 0.3 mmol / g or more and 0.85 mmol / g or less.
The carboxy group concentration A1 of the amorphous vinyl polymer A and the carboxy group concentration B1 of the amorphous vinyl polymer B preferably satisfy the following relational expressions (1) and (2).
Relational expression (1): B1 <A1
Relational expression (2): A1-B1 ≦ | 0.5 |
When the carboxy group concentration A1 of the amorphous vinyl polymer A and the carboxy group concentration B1 of the amorphous vinyl polymer B satisfy the relational expressions (1) and (2), the amorphous vinyl polymer A and Amorphous vinyl polymer A exhibits higher hydrophilicity while amorphous vinyl polymer A exhibits higher hydrophilicity. Therefore, when producing toner in an aqueous medium, amorphous vinyl polymer The fine particles of A (main resin) are formed while the composite fine particles are efficiently taken into the inside, and the resulting toner has charging performance while having even higher low-temperature fixability and heat-resistant storage stability. Long-term stability is sufficiently obtained.
When the carboxy group concentration A1 of the amorphous vinyl polymer A is less than or equal to the carboxy group concentration B1 of the amorphous vinyl polymer B (B1 ≧ A1), the composite fine particles are not produced during toner production in an aqueous medium. There is a possibility that particles are formed while being exposed on the surface of the toner particles to be formed, and there is a possibility that long-term stability of sufficient charging performance may not be obtained in the obtained toner.
When the difference between the carboxy group concentration A1 of the amorphous vinyl polymer A and the carboxy group concentration B1 of the amorphous vinyl polymer B is greater than 0.5, the amorphous vinyl polymer A and the amorphous vinyl polymer A A sufficiently high affinity with the conductive vinyl polymer B cannot be obtained, and the fine particles of the amorphous vinyl polymer A may not be able to efficiently take in the composite fine particles during the production of toner in an aqueous medium. .

  In the toner of the present invention, the binder resin may contain other resins in addition to the amorphous vinyl polymer constituting the matrix phase and the crystalline polyester resin constituting the domain phase.

[Colorant]
In the toner of the present invention, when the toner particles are configured to contain a colorant, the colorant may be contained in either the matrix phase or the domain phase, but from the viewpoint of dispersibility of the colorant. In particular, it is preferable to be contained in the matrix phase.
Examples of carbon black include channel black, furnace black, acetylene black, thermal black, and lamp black. Examples of black iron oxide include magnetite, hematite, and iron iron trioxide.
Examples of the dye include C.I. I. Solvent Red 1, 49, 52, 58, 63, 111, 122, C.I. I. Solvent Yellow 19, 44, 77, 79, 81, 82, 93, 98, 103, 104, 112, 162, C.I. I. Solvent Blue 25, 36, 60, 70, 93, 95 and the like.
Examples of the pigment include C.I. I. Pigment Red 5, 48: 1, 48: 3, 53: 1, 57: 1, 81: 4, 122, 139, 144, 149, 150, 166, 177, 178, 222, 238, 269, C.I. I. Pigment Orange 31 and 43, C.I. I. Pigment yellow 14, 17, 74, 93, 94, 138, 155, 156, 158, 180, 185, C.I. I. Pigment green 7, C.I. I. Pigment Blue 15: 3, 60, and the like.
The colorant for obtaining the toner of each color can be used singly or in combination of two or more for each color.

  The content ratio of the colorant is preferably 1 to 10% by mass in the toner particles, and more preferably 2 to 8% by mass. If the content of the colorant is too small, the resulting toner may not have the desired coloring power. On the other hand, if the content of the colorant is excessive, it may be released to the colorant or to the carrier. May occur, which may affect the chargeability.

〔Release agent〕
In the toner of the present invention, when the toner particles are configured to contain a release agent, the release agent may be contained in either the matrix phase or the domain phase. From the viewpoint of surface oozing out, it is particularly preferable that it is contained in the matrix phase.
As the wax, polyolefin waxes such as low molecular weight polypropylene, polyethylene, or oxidized polypropylene, polyethylene, and ester waxes such as behenate behenate can be preferably used.
Specifically, polyolefin waxes such as polyethylene wax and polypropylene wax; branched hydrocarbon waxes such as microcrystalline wax; long-chain hydrocarbon waxes such as paraffin wax and sazol wax; dialkyls such as distearyl ketone Ketone wax; carnauba wax, montan wax, behenate behenate, trimethylolpropane tribehenate, pentaerythritol tetrabehenate, pentaerythritol diacetate dibehenate, glycerin tribehenate, 1,18-octadecanediol di Ester wax such as stearate, trimellitic trimellitic acid, distearyl maleate; ethylenediamine behenylamide, trimellitic acid tristearylamide Such as amide waxes.
Among these, from the viewpoint of releasability during low-temperature fixing, it is preferable to use those having a low melting point, specifically, those having a melting point of 40 to 90 ° C.

  The content ratio of the release agent is preferably 1 to 20% by mass in the toner particles, and more preferably 5 to 20% by mass. When the content ratio of the release agent in the toner particles is in the above range, both the separation property and the fixing property can be reliably obtained.

[Charge control agent]
In the toner of the present invention, when the toner particles are configured to contain a charge control agent, the charge control agent may be contained in either the matrix phase or the domain phase. From the viewpoint of the above, it is particularly preferable that it is contained in the matrix phase.
The content ratio of the charge control agent is usually 0.1 to 10 parts by mass, preferably 0.5 to 5 parts by mass with respect to 100 parts by mass of the finally obtained binder resin.

(External additive)
In the toner of the present invention, the toner particles can be used as toners as they are. However, in order to improve fluidity, chargeability, cleaning properties, etc., the toner particles may contain so-called fluidizing agents, cleaning aids, etc. An external additive may be added.
Various external additives may be used in combination.
The total addition amount of these external additives is preferably 0.05 to 5 parts by mass, more preferably 0.1 to 3 parts by mass with respect to 100 parts by mass of the toner particles.

[Toner glass transition point]
The toner of the present invention preferably has a glass transition point (Tg) of 25 to 50 ° C, more preferably 35 to 55 ° C.
When the glass transition point of the toner of the present invention is in the above range, sufficient low-temperature fixing property and heat-resistant storage property can be surely achieved. When the glass transition point of the toner is too small, the heat resistance (thermal strength) of the toner is lowered, and there is a possibility that sufficient heat storage stability and hot offset resistance cannot be obtained. Further, when the glass transition point of the toner is excessive, there is a possibility that sufficient low-temperature fixability cannot be obtained.

  The glass transition point of the toner is measured in the same manner as described above except that the toner is used as a measurement sample.

[Toner particle size]
In the toner of the present invention, the average particle diameter is preferably 3 to 8 μm, and more preferably 5 to 8 μm, for example, on a volume basis median diameter. This average particle size can be controlled by the concentration of the flocculant used during production, the amount of organic solvent added, the fusing time, the composition of the binder resin, and the like.
When the volume-based median diameter is in the above range, a very small dot image of 1200 dpi level can be faithfully reproduced.

  The volume-based median diameter of the toner is measured and calculated using a measuring apparatus in which a computer system equipped with data processing software “Software V3.51” is connected to “Multisizer 3” (manufactured by Beckman Coulter). Is. Specifically, 0.02 g of a measurement sample (toner) was added to 20 mL of a surfactant solution (for example, a surfactant obtained by diluting a neutral detergent containing a surfactant component 10 times with pure water for the purpose of dispersing toner particles). After adding the solution to the solution), ultrasonic dispersion is performed for 1 minute to prepare a toner dispersion, and this toner dispersion is added to a beaker containing “ISOTONII” (manufactured by Beckman Coulter) in a sample stand. Then, inject with a pipette until the displayed concentration of the measuring device is 8%. Here, a reproducible measurement value can be obtained by setting the concentration range. In the measuring apparatus, the measurement particle count number is 25000, the aperture diameter is 100 μm, and the frequency value is calculated by dividing the range of 2 to 60 μm, which is the measurement range, into 256 parts. % Particle diameter is defined as the volume-based median diameter.

[Average circularity of toner]
In the toner of the present invention, the individual toner particles constituting the toner preferably have an average circularity of 0.930 to 1.000 from the viewpoints of stability of charging characteristics and low-temperature fixability. More preferably, it is 950 to 0.995.
When the average circularity is within the above range, the individual toner particles are less likely to be crushed, the contamination of the frictional charge imparting member is suppressed, the toner chargeability is stabilized, and the image quality of the formed image is high. It will be a thing.

The average circularity of the toner is a value measured using “FPIA-2100” (manufactured by Sysmex). Specifically, the measurement sample (toner) was blended with an aqueous solution containing a surfactant, dispersed by performing ultrasonic dispersion for 1 minute, and then subjected to measurement conditions HPF by “FPIA-2100” (manufactured by Sysmex). In the (high magnification imaging) mode, photographing is performed at an appropriate density of 3,000 to 10,000 HPF detections, and the circularity of each toner particle is calculated according to the following formula (y). This is a value calculated by adding the degree and dividing by the total number of toner particles. If the number of HPF detections is in the above range, reproducibility can be obtained.
Formula (y): Circularity = (perimeter of a circle having the same projection area as the particle image) / (perimeter of the particle projection image)

(Developer)
The toner of the present invention can be used as a magnetic or non-magnetic one-component developer, but may be mixed with a carrier and used as a two-component developer. When the toner is used as a two-component developer, the carrier includes magnetic particles made of conventionally known materials such as metals such as iron, ferrite and magnetite, and alloys of these metals with metals such as aluminum and lead. In particular, ferrite particles are preferable. Further, as the carrier, a coated carrier in which the surface of magnetic particles is coated with a coating agent such as a resin, a dispersion type carrier in which a magnetic fine powder is dispersed in a binder resin, or the like may be used.
The volume-based median diameter of the carrier is preferably 20 to 100 μm, more preferably 25 to 80 μm. The volume-based median diameter of the carrier can be typically measured by a laser diffraction particle size distribution measuring apparatus “HELOS” (manufactured by SYMPATEC) equipped with a wet disperser.

[Toner Production Method]
The method for producing the toner of the present invention is not particularly limited, and examples thereof include a wet production method prepared in an aqueous medium, such as an emulsion aggregation method.
The method for producing the toner of the present invention by the emulsion aggregation method includes an aqueous dispersion in which fine particles of a binder resin (hereinafter also referred to as “binder resin fine particles”) are dispersed in an aqueous medium, and fine particles of a colorant ( (Hereinafter also referred to as “colorant fine particles”) is mixed with an aqueous dispersion, and the toner particles are formed by aggregating and thermally fusing the binder resin fine particles and the colorant fine particles.
The binder resin fine particles may have a multilayer structure of two or more layers made of binder resins having different compositions. For example, a binder resin fine particle having such a structure has a two-layer structure. A dispersion of resin particles is prepared by a polymerization treatment according to the method (first-stage polymerization), a polymerization initiator and a polymerizable monomer are added to the dispersion, and this system is polymerized (second-stage polymerization). ).

  Here, the “aqueous dispersion” is a dispersion in which a dispersion (fine particles) is dispersed in an aqueous medium, and the aqueous medium is one in which a main component (50% by mass or more) is water. . Examples of components other than water include organic solvents that dissolve in water, such as methanol, ethanol, isopropanol, butanol, acetone, methyl ethyl ketone, and tetrahydrofuran. Among these, alcohol-based organic solvents such as methanol, ethanol, isopropanol, and butanol, which are organic solvents that do not dissolve the resin, are particularly preferable.

An example of a method for producing the toner of the present invention is specifically shown as follows:
(A) a step of preparing an aqueous dispersion in which fine particles of amorphous vinyl polymer A (hereinafter also referred to as “resin fine particles (A)”) are dispersed in an aqueous medium;
(B) A crystalline polyester resin obtained by adding a vinyl monomer to an aqueous dispersion in which fine particles of a crystalline polyester resin (hereinafter also referred to as “crystalline polyester resin fine particles”) are dispersed in an aqueous medium. By carrying out seed polymerization with a vinyl monomer using the fine particles as seeds, an aqueous dispersion is prepared in which composite fine particles in which the amorphous vinyl polymer B is adhered to the surface of the crystalline polyester resin fine particles are dispersed. Process,
(C) a step of preparing an aqueous dispersion in which colorant fine particles are dispersed in an aqueous medium;
(D) a step of aggregating and fusing the resin fine particles (A), composite fine particles and colorant fine particles in an aqueous medium to form associated particles;
(E) aging associated particles with thermal energy to control the shape and obtaining toner particles (f) cooling the toner particle dispersion;
(G) a step of filtering the toner particles from the aqueous medium and removing the surfactant from the toner particles;
(H) It consists of steps such as drying the washed toner particles, and if necessary,
(I) A step of adding an external additive to the dried toner particles can be added.

(A) Preparation Step of Aqueous Dispersion of Resin Fine Particles (A) In this step, an aqueous dispersion of resin fine particles (A) with amorphous vinyl polymer A is prepared.
The aqueous dispersion of the resin fine particles (A) can be prepared by a miniemulsion polymerization method using a vinyl monomer for obtaining the amorphous vinyl polymer A. That is, for example, a vinyl monomer is added to an aqueous medium containing a surfactant, mechanical energy is applied to form droplets, and then the droplets are formed by radicals from a water-soluble radical polymerization initiator. The polymerization reaction proceeds inside. Note that an oil-soluble polymerization initiator may be contained in the droplet. Thereby, the aqueous dispersion of the resin fine particles (A) by the amorphous vinyl polymer A can be prepared.

[Surfactant]
As the surfactant used in this step, conventionally known various anionic surfactants, cationic surfactants, nonionic surfactants and the like can be used.

(Polymerization initiator)
As the polymerization initiator used in this step, various conventionally known polymerization initiators can be used. As specific examples of the polymerization initiator, for example, persulfates (potassium persulfate, ammonium persulfate, etc.) are preferably used. In addition, azo compounds (4,4′-azobis-4-cyanovaleric acid and its salts, 2,2′-azobis (2-amidinopropane) salts, etc.), peroxide compounds, azobisisobutyronitrile, etc. Also good.

[Chain transfer agent]
In this step, a generally used chain transfer agent can be used for the purpose of adjusting the molecular weight of the amorphous vinyl polymer A. The chain transfer agent is not particularly limited, and examples thereof include mercaptans such as 2-chloroethanol, octyl mercaptan, dodecyl mercaptan, and t-dodecyl mercaptan, and styrene dimers.

The toner particles according to the present invention may contain, in addition to the binder resin, other internal additives such as a release agent and a charge control agent as necessary. In this step, for example, can be introduced into the toner particles by dissolving or dispersing in advance in a solution of a vinyl monomer for forming the amorphous vinyl polymer A.
In addition, such an internal additive is prepared by separately preparing a dispersion of internal additive fine particles consisting only of the internal additive, and the internal additive together with the resin fine particles (A), composite fine particles and colorant fine particles in the aggregation / fusion process. Although it is possible to introduce the toner particles into the toner particles by aggregating the agent fine particles, it is preferable to adopt a method of introducing them in advance in this step.

The average particle diameter of the resin fine particles (A) is preferably in the range of 20 to 400 nm in terms of volume-based median diameter.
In the present invention, the volume-based median diameter of the resin fine particles is a value measured using “Microtrac UPA-150” (manufactured by Nikkiso Co., Ltd.).

(B) Step of preparing aqueous dispersion of composite fine particles In this step, composite fine particles in which amorphous vinyl polymer B formed by using a vinyl monomer is attached to the surface of crystalline polyester resin fine particles. An aqueous dispersion is prepared.
Specifically, a crystalline polyester resin is synthesized, the crystalline polyester resin is dispersed in the form of fine particles in an aqueous medium to obtain an aqueous dispersion in which the crystalline polyester resin fine particles are dispersed, and the aqueous dispersion is obtained. Then, an aqueous dispersion of composite fine particles can be prepared by adding a vinyl monomer and a polymerization initiator and performing seed polymerization with a vinyl monomer using the crystalline polyester resin fine particles as a seed.

An aqueous dispersion of crystalline polyester resin fine particles is prepared by dissolving or dispersing a crystalline polyester resin in an organic solvent to prepare an oil phase liquid, and dispersing the oil phase liquid in an aqueous medium by phase inversion emulsification or the like. After forming oil droplets in a state of being controlled to a desired particle size, it can be prepared by removing the organic solvent.
The amount of the aqueous medium used is preferably 50 to 2,000 parts by mass and more preferably 100 to 1,000 parts by mass with respect to 100 parts by mass of the oil phase liquid.
A surfactant or the like may be added to the aqueous medium for the purpose of improving the dispersion stability of the oil droplets. As surfactant, the thing similar to what was mentioned in said process can be mentioned.

The organic solvent used for the preparation of the oil phase liquid is preferably one having a low boiling point and low solubility in water from the viewpoint of easy removal treatment after formation of oil droplets. Examples thereof include methyl acetate, ethyl acetate, methyl ethyl ketone, methyl isobutyl ketone, toluene, xylene and the like. These can be used alone or in combination of two or more. The usage-amount of an organic solvent is 1-300 mass parts normally with respect to 100 mass parts of crystalline polyester resins.
The emulsification and dispersion of the oil phase liquid can be performed using mechanical energy.

The average particle diameter of the crystalline polyester resin fine particles used as a seed is preferably in the range of 10 to 400 nm in terms of volume-based median diameter.
In the present invention, the volume-based median diameter of the crystalline polyester resin fine particles is a value measured using “Microtrack UPA-150” (manufactured by Nikkiso Co., Ltd.).

  In the seed polymerization, a generally used chain transfer agent can be used for the purpose of adjusting the molecular weight of the amorphous vinyl polymer B. Examples of the chain transfer agent include the same ones as mentioned in the above step.

  As a polymerization initiator, the thing similar to what was mentioned in said process can be mentioned.

  The seed polymerization is preferably performed in a state where the viscosity of the crystalline polyester resin is high, and the polymerization temperature of the seed polymerization is preferably the melting point of the crystalline polyester resin + 20 ° C. or less, and the melting point + 10 ° C. or less. Is more preferable, and it is still more preferable that it is below melting | fusing point.

The average particle diameter of the composite fine particles is preferably in the range of 20 to 400 nm in terms of volume-based median diameter.
In the present invention, the volume-based median diameter of the composite fine particles is a value measured using “Microtrac UPA-150” (manufactured by Nikkiso Co., Ltd.).

(C) Preparation Step of Aqueous Dispersion of Colorant Fine Particles This step is a step that is performed as necessary when toner particles containing a colorant are desired, and the colorant is finely divided in an aqueous medium. In which an aqueous dispersion of fine colorant particles is prepared.

The aqueous dispersion of colorant fine particles can be obtained by dispersing the colorant in an aqueous medium in which a surfactant is added to a critical micelle concentration (CMC) or higher.
The colorant can be dispersed using mechanical energy, and the disperser to be used is not particularly limited. However, an ultrasonic disperser, a mechanical homogenizer, a manton gourin or a pressure homogenizer is preferably used. Examples thereof include medium dispersers such as a pressure disperser, a sand grinder, a Getzman mill, and a diamond fine mill.

The colorant fine particles preferably have a volume-based median diameter of 10 to 300 nm in a dispersed state, more preferably 100 to 200 nm, and particularly preferably 100 to 150 nm.
In the present invention, the volume-based median diameter of the colorant fine particles is a value measured using an electrophoretic light scattering photometer “ELS-800” (manufactured by Otsuka Electronics Co., Ltd.).

(D) Aggregation / fusion step In this step, the resin fine particles (A), the composite fine particles and the colorant fine particles, and if necessary, the fine particles of other toner constituents are aggregated and further fused by heating.
Specifically, an amorphous vinyl polymer A and an amorphous vinyl polymer B glass are added by adding an aggregating agent having a critical aggregation concentration or higher to an aqueous dispersion obtained by dispersing the above fine particles in an aqueous medium. Aggregation and fusion are performed by setting the temperature to a temperature higher than the transition point.

In this step, the flocculant is added to the aqueous medium in which the resin fine particles (A) and the colorant fine particles are dispersed in a state below the glass transition point of the amorphous vinyl polymer A and the amorphous vinyl polymer B. After the addition, it is preferable to add the composite fine particles without raising the temperature. In particular, the aggregated particles in which the resin fine particles (A) and the colorant fine particles are aggregated are 1 / of the particle size of the toner particles to be formed. When the size becomes 4 to 1/2, it is preferable to add composite fine particles and then raise the temperature to the glass transition point of amorphous vinyl polymer A and amorphous vinyl polymer B or higher.
By adding the composite fine particles at such timing and subjecting them to aggregation, the composite fine particles can be confined inside the toner particles to be formed.

  The fusing temperature for fusing the resin fine particles (A) and the composite fine particles may be at least the glass transition point of the amorphous vinyl polymer A and the amorphous vinyl polymer B. Glass transition point of crystalline vinyl polymer A and amorphous vinyl polymer B + 10 ° C.) to (amorphous vinyl polymer A and amorphous vinyl polymer B + 50 ° C.), particularly preferably (amorphous The glass transition point of vinyl polymer A and amorphous vinyl polymer B + 15 ° C.) to (the glass transition point of amorphous vinyl polymer A and amorphous vinyl polymer B + 40 ° C.).

[Flocculant]
The flocculant used in this step is not particularly limited, but those selected from metal salts such as alkali metal salts and alkaline earth metal salts are preferably used. Examples of the metal salt include monovalent metal salts such as sodium, potassium, and lithium; divalent metal salts such as calcium, magnesium, manganese, and copper; and trivalent metal salts such as iron and aluminum. Specific metal salts can include sodium chloride, potassium chloride, lithium chloride, calcium chloride, magnesium chloride, zinc chloride, copper sulfate, magnesium sulfate, manganese sulfate, and the like. It is particularly preferable to use a divalent metal salt. These can be used individually by 1 type or in combination of 2 or more types.

(E) Aging step This step is carried out as necessary, and in this aging step, the associated particles obtained by the aggregation / fusion step are aged to a desired shape by heat energy. An aging process for forming toner particles is performed.
Specifically, the aging treatment is performed by adjusting the heating temperature, stirring speed, heating time, and the like until the shape of the associated particles reaches a desired circularity by heating and stirring the system in which the associated particles are dispersed. Done.

(F) Cooling Step This step is a step of cooling the toner particle dispersion. As a condition for the cooling treatment, it is preferable to cool at a cooling rate of 1 to 20 ° C./min. The specific method of the cooling treatment is not particularly limited, and examples include a method of cooling by introducing a refrigerant from the outside of the reaction vessel, a method of cooling by directly introducing cold water into the reaction system, and the like. it can.

(G) Filtration / Washing Step This step involves solid-liquid separation of the toner particles from the cooled dispersion of toner particles, and a toner cake obtained by solid-liquid separation (aggregating toner particles in a wet state into a cake form) This is a step of removing adhering substances such as a surfactant and an aggregating agent from the aggregate).
The solid-liquid separation is not particularly limited, and a centrifugal separation method, a vacuum filtration method using Nutsche or the like, a filtration method using a filter press, or the like can be used. Further, in washing, it is preferable to wash with water until the electric conductivity of the filtrate reaches 10 μS / cm.

(H) Drying Step This step is a step of drying the washed toner cake, and can be carried out according to a drying step in a generally known method for producing toner particles.
Specifically, examples of the dryer used for drying the toner cake include a spray dryer, a vacuum freeze dryer, and a vacuum dryer, and a stationary shelf dryer, a mobile shelf dryer, a fluidized bed, and the like. It is preferable to use a dryer, a rotary dryer, a stirring dryer or the like.
The moisture of the dried toner particles is preferably 5% by mass or less, more preferably 2% by mass or less. In addition, when the dried toner particles are aggregated by a weak interparticle attractive force, the aggregate may be crushed. Here, as the crushing treatment apparatus, a mechanical crushing apparatus such as a jet mill, a Henschel mixer, a coffee mill, or a food processor can be used.

(I) External additive addition step This step is a step that is performed as necessary when an external additive is added to the toner particles.
The above toner particles can be used as toners as they are, but in order to improve fluidity, chargeability, cleaning properties, etc., external additives such as fluidizing agents and cleaning aids are added to the toner particles. You may use it in the state.
Various external additives may be used in combination.
The total addition amount of these external additives is preferably 0.05 to 5 parts by mass, more preferably 0.1 to 3 parts by mass with respect to 100 parts by mass of the toner particles.
As the external additive mixing device, a mechanical mixing device such as a Henschel mixer or a coffee mill can be used.

  According to the above toner, the binder resin has a domain matrix structure, and the carboxy group concentration of the amorphous vinyl polymer constituting the matrix phase and the ester group concentration of the crystalline polyester resin constituting the domain phase are By being in a specific range, heat-resistant storage stability can be obtained while having low-temperature fixability and long-term stability of charging performance.

Although the embodiments of the present invention have been specifically described above, the embodiments of the present invention are not limited to the above examples, and various modifications can be made.
For example, the toner of the present invention may be composed of toner particles having a core-shell structure including core particles containing a binder resin and a shell layer made of a shell resin covering the outer peripheral surface thereof.
According to the toner in which the shell layer is formed in this way, the crystalline polyester resin constituting the domain phase is not exposed on the surface of the toner particles, and therefore the crystalline polyester resin exists on the surface of the toner particles. It is possible to further suppress the deterioration of the charging performance due to.

  Here, the “core-shell structure” may be not only a form in which the shell layer completely covers the core particles but also a part of the core particles. Further, a part of the shell resin constituting the shell layer may form a domain or the like in the core particle. Further, the shell layer may have a multilayer structure of two or more layers made of resins having different compositions.

Hereinafter, specific examples of the present invention will be described, but the present invention is not limited thereto.
The measurement of the volume-based median diameter of the resin fine particles, the colorant fine particles, the crystalline polyester resin fine particles, and the composite fine particles, and the measurement of the molecular weight of the resin fine particles and the crystalline polyester resin were performed as described above.
Further, the measurement of the glass transition point (Tg) of the resin fine particles and the toner and the measurement of the melting point of the crystalline polyester resin were performed as described above.

[Preparation Example 1 of aqueous dispersion of resin fine particles]
(First stage polymerization)
A 5 L reaction vessel equipped with a stirrer, a temperature sensor, a cooling pipe and a nitrogen introducing device was charged with a solution prepared by dissolving 8 g of sodium dodecyl sulfate in 3 L of ion-exchanged water, and stirred at a stirring speed of 230 rpm under a nitrogen stream. After the internal temperature was raised to 80 ° C., a solution in which 10 g of potassium persulfate was dissolved in 200 g of ion-exchanged water was added, the liquid temperature was again adjusted to 80 ° C., 480 g of styrene, 250 g of n-butyl acrylate and 68 g of methacrylic acid. After the monomer mixture consisting of 1 was added dropwise over 1 hour, polymerization was carried out by heating and stirring at 80 ° C. for 2 hours to prepare an aqueous dispersion [a1] in which resin fine particles [a1] were dispersed.

(Second stage polymerization)
A 5 L reaction vessel equipped with a stirrer, temperature sensor, cooling tube and nitrogen introducing device was charged with a solution of 7 g of polyoxyethylene (2) sodium dodecyl ether sulfate in 800 ml of ion-exchanged water and heated to 98 ° C. 90 g of the above resin fine particles [a1] 260 g, styrene 137 g, n-butyl acrylate 70 g, n-octyl-3-mercaptopropionate 1.0 g and release agent (behenate behenate (melting point 73 ° C.)) 90 g The monomer mixture dissolved and mixed at 0 ° C. is added and mixed and dispersed for 1 hour by a mechanical disperser “CREARMIX” (manufactured by M Technique Co., Ltd.) having a circulation path. A dispersion containing was prepared.
Next, an initiator solution in which 6 g of potassium persulfate is dissolved in 200 ml of ion-exchanged water is added to this dispersion, and the system is polymerized by heating and stirring at 82 ° C. for 1 hour to obtain resin fine particles [a2]. A water-based dispersion liquid [a2] in which is dispersed is prepared.

(3rd stage polymerization)
A solution prepared by dissolving 11 g of potassium persulfate in 400 ml of ion-exchanged water was added to the aqueous dispersion [a2], and 241 g of styrene, 78 g of n-butyl acrylate, 28 g of methacrylic acid, A monomer mixture composed of 28 g of methyl acid and 6 g of n-octyl-3-mercaptopropionate was added dropwise over 1 hour. After completion of the dropwise addition, polymerization was carried out by heating and stirring for 2 hours, followed by cooling to 28 ° C., thereby preparing an aqueous dispersion [A1] of resin fine particles [A1] with an amorphous vinyl polymer.
With respect to this aqueous dispersion [A1], the volume-based median diameter of the resin fine particles [A1] was 220 nm, the weight average molecular weight (Mw) was 35,000, and the glass transition point (Tg) was 52 ° C.

[Preparation Examples 2-7 of aqueous dispersions of resin fine particles]
Resin fine particles [A2] to [A2] to [A] are prepared in the same manner as in Preparation Example 1 of the aqueous dispersion of resin fine particles, except that the addition amount of the monomer is changed so that the resin composition has the molar ratio shown in Table 1. A7] aqueous dispersions [A2] to [A7] were prepared.

[Synthesis Example 1 of crystalline polyester resin]
In a 5 L reaction vessel equipped with a stirrer, a temperature sensor, a cooling pipe and a nitrogen introducing device, 300 parts by mass of polycarboxylic acid: sebacic acid (molecular weight 202.25) and polyhydric alcohol: 1,6-hexanediol ( The molecular weight was 118.17) and 170 parts by mass were charged. While stirring this system, the internal temperature was raised to 190 ° C. over 1 hour. After confirming that the system was uniformly stirred, Ti was used as the catalyst. (OBu) ₄ was added in an amount of 0.003% by mass relative to the charged amount of the polyvalent carboxylic acid compound. Thereafter, the internal temperature is raised from 190 ° C. to 240 ° C. over 6 hours while distilling off the generated water, and the dehydration condensation reaction is continued over 6 hours under the condition of a temperature of 240 ° C. for polymerization. As a result, a crystalline polyester resin [C1] was obtained.
The crystalline polyester resin [C1] obtained had a melting point (Tm) of 66.8 ° C. and a number average molecular weight (Mn) of 6,300.

[Synthetic Examples 2 to 6 of crystalline polyester resin]
Crystalline polyester resins [C2] to [C6] were synthesized in the same manner as in Synthesis Example 1 of Crystalline Polyester Resin, except that the type and amount of monomer were changed according to Table 2.

[Preparation Example 1 of aqueous dispersion of crystalline polyester resin fine particles]
30 parts by mass of the crystalline polyester resin [C1] was melted and transferred in the molten state to the emulsification disperser “Cabitron CD1010” (manufactured by Eurotech Co., Ltd.) at a transfer rate of 100 parts by mass. Simultaneously with the transfer of the crystalline polyester resin [C1] in the molten state, 70 mass parts of reagent ammonia water was diluted with ion-exchanged water in an aqueous solvent tank with respect to the emulsification disperser, and the concentration was 0.37 mass%. The diluted ammonia water was transferred at a transfer rate of 0.1 liter per minute while being heated to 100 ° C. with a heat exchanger. Then, by operating this emulsification disperser under the conditions of a rotor rotation speed of 60 Hz and a pressure of 5 kg / cm ² , crystalline polyester resin fine particles having a volume-based median diameter of 200 nm and a solid content of 30 parts by mass [ An aqueous dispersion [C1] of C1] was prepared.

[Preparation Examples 2-6 of Aqueous Dispersion of Crystalline Polyester Resin Fine Particles]
In the preparation example 1 of the aqueous dispersion of crystalline polyester resin fine particles, the crystalline polyester resin [C2] to [C6] was used instead of the crystalline polyester resin [C1], respectively. Aqueous dispersions [C2] to [C6] of resin fine particles [C2] to [C6] were prepared.

[Preparation Example 1 of aqueous dispersion of composite fine particles]
Into a 5 L reaction vessel equipped with a stirrer, a temperature sensor, a cooling pipe and a nitrogen introducing device, 2000 parts by mass of an aqueous dispersion [C1] of crystalline polyester resin fine particles [C1] and 1150 parts by mass of ion-exchanged water were charged. Further, a polymerization initiator solution in which 10.3 parts by mass of potassium persulfate was dissolved in 210 parts by mass of ion-exchanged water was added. Under a temperature condition of 80 ° C., styrene ( (St) 390 parts by mass, n-butyl acrylate (BA) 143 parts by mass, methacrylic acid (MAA) 27 parts by mass and methyl methacrylate (MMA) 40 parts by mass were dropped over 2 hours, The seed polymerization is carried out by heating and stirring at 80 ° C. for 2 hours. After the polymerization is completed, the crystalline polymer is cooled to 28 ° C. To prepare an aqueous dispersion [S1] of the composite fine particles (S1) for containing the ester resin fine particles [C1].
With respect to this aqueous dispersion [S1], the volume-based median diameter of the composite fine particles [S1] was 280 nm.

[Preparation Examples 2 to 8 of aqueous dispersions of composite fine particles]
In Preparation Example 1 of the aqueous dispersion of composite fine particles, the amount of monomer added was changed so that the resin composition of the coating resin was as shown in Table 3 in terms of molar ratio, and the seed used (crystalline polyester resin fine particles) In the same manner, except that the amount of the aqueous dispersion was changed so that the content ratio of the coating resin and the seed was as shown in Table 3 in terms of mass ratio. Thus, aqueous dispersions [S2] to [S8] of the composite fine particles [S2] to [S8] were prepared.

[Preparation Example 1 of Aqueous Dispersion of Colorant Fine Particles]
90 parts by mass of sodium polyoxyethylene-2-dodecyl ether sulfate was stirred and dissolved in 1510 parts by mass of ion-exchanged water. While stirring this solution, 400 parts by mass of carbon black “Regal 330” (manufactured by Cabot) is gradually added, and then dispersed using a stirrer “Claremix” (manufactured by M Technique). Thus, an aqueous dispersion [Bk] of fine colorant particles was prepared.
The volume-based median diameter of the colorant fine particles in the aqueous dispersion [Bk] of the colorant fine particles was measured and found to be 110 nm.

<Toner Production Example 1>
In a zebra flask equipped with a stirrer, a temperature sensor, a cooling tube, and a nitrogen introducing device, 2500 parts by mass of ion exchange water, 600 parts by mass of an aqueous dispersion [A1] of resin fine particles [A1] (in terms of solid content), composite fine particles [ S1] aqueous dispersion [S1] 300 parts by mass (in terms of solid content) and colorant fine particles [Bk] aqueous dispersion [Bk] 500 parts by mass were prepared, and the liquid temperature was adjusted to 25 ° C. The pH was adjusted to 10 by adding 25% by weight aqueous sodium hydroxide solution.
Next, an aqueous solution in which 54.3 parts by mass of magnesium chloride hexahydrate is dissolved in 54.3 parts by mass of ion-exchanged water is added, and then the temperature of the system is raised to 97 ° C. to thereby form each resin fine particle. And agglomeration reaction of the colorant fine particles was started.
After the start of this agglomeration reaction, sampling is performed periodically, and the volume-based median diameter of the particles is measured using a particle size distribution analyzer “Coulter Multisizer 3” (manufactured by Beckman Coulter). Aggregation was continued while stirring was continued until 6.3 μm.
Thereafter, an aqueous solution in which 23.0 parts by mass of sodium chloride was dissolved in 92 parts by mass of ion-exchanged water was added, the temperature of the system was kept at 95 ° C., and stirring was continued for 4 hours, and a flow-type particle image analyzer “FPIA-2100” When the circularity reached 0.946 as measured by (Sysmex), the reaction was stopped by cooling to 30 ° C. under conditions of 6 ° C./min to obtain a dispersion of toner particles. The toner particles after cooling had a particle size of 6.1 μm and a circularity of 0.946.
The toner particle dispersion thus obtained was subjected to solid-liquid separation using a basket-type centrifuge “MARK III Model No. 60 × 40” (manufactured by Matsumoto Kikai Co., Ltd.) to form a wet cake. This wet cake was repeatedly washed and solid-liquid separated with the basket-type centrifuge until the electric conductivity of the filtrate reached 15 μS / cm. Thereafter, a “flash jet dryer” (manufactured by Seishin Enterprise Co., Ltd.) was used, and the temperature was 40 The toner particles [1] were obtained by spraying a stream of air at a temperature of 20 ° C. and a humidity of 20% RH until the water content was 0.5 mass% and cooling to 24 ° C.

To the obtained toner particles [1], 1% by mass of hydrophobic silica particles and 1.2% by mass of hydrophobic titanium oxide particles are added, and the condition of the peripheral speed of the rotor blades is 24 m / s using a Henschel mixer. Was added for 20 minutes, and an external additive was added by passing through a 400 mesh sieve to obtain toner [1].
It was 37 degreeC when the glass transition point was measured about the obtained toner [1].
In toner [1], the shape and particle size of the toner particles did not change with the addition of hydrophobic silica particles and hydrophobic titanium oxide particles.

[Toner Production Examples 2 to 14]
In Toner Production Example 1, the types of the aqueous dispersion [A1] of the resin fine particles [A1] and the aqueous dispersion [S1] of the composite fine particles [S1] were changed as shown in Table 4, and each resin Toners [2] to [14] were obtained in the same manner except that the addition amount of the aqueous dispersion was changed so that the content ratio was as shown in Table 4 in terms of mass ratio.
The toner [8] was prepared using an aqueous dispersion [C2] of crystalline polyester resin fine particles [C2] instead of the aqueous dispersion [S1] of the composite fine particles [S1]. In the toner [13], an aqueous dispersion [X] of amorphous polyester resin fine particles [X] shown below is used in place of the aqueous dispersion [A1] of resin fine particles [A1], and composite fine particles [X] are used. It was prepared using an aqueous dispersion [C2] of crystalline polyester resin fine particles [C2] instead of the aqueous dispersion [S1] of S1. Further, the toner [14] was prepared without adding the aqueous dispersion [S1] of the composite fine particles [S1].

[Preparation Example of Aqueous Dispersion of Amorphous Polyester Resin Fine Particles]
(1) Synthesis of amorphous polyester resin 525 parts by mass of bisphenol A propylene oxide 2 mol adduct, 225 parts by mass of bisphenol A ethylene oxide 2 mol adduct, 375 parts by mass of terephthalic acid, 20 parts by mass of fumaric acid, branched structure 120 parts by mass of dodecenyl succinic acid (succinic acid 1) having a proportion of dodecenyl succinic acid (3 carbon atoms in the branched portion) of 15 mol%, and 2 mol of dodecenyl succinic acid having a branched structure (3 carbon atoms in the branched portion) After adding 180 parts by mass of dodecenyl succinic acid (succinic acid 2) and 6 parts by mass of dibutyltin oxide to a heat-dried three-necked flask, the pressure in the container is reduced by a vacuum operation, and further inert by nitrogen gas The reaction was carried out at 230 ° C and normal pressure (101.3 kPa) for 10 hours with mechanical stirring under an atmosphere. The mixture was further reacted at 8 kPa for 1 hour. After cooling to 210 ° C. and adding 75 parts by mass of trimellitic anhydride and reacting for 1 hour, the reaction was continued at 8 kPa until the softening temperature became 120 ° C. to obtain amorphous polyester resin [X].
(2) Preparation of Aqueous Dispersion of Amorphous Polyester Resin Fine Particles Next, 350 parts by mass of amorphous polyester resin [X] after removing insolubles, 245 parts by mass of methyl ethyl ketone, 70 parts by mass of isopropyl alcohol, 10 After 11.2 parts by mass of a mass% aqueous ammonia solution is placed in a separable flask, mixed and dissolved, ion-exchanged water is dropped at a liquid feed rate of 8 g / min using a liquid feed pump while stirring at 40 ° C. did. After the liquid became cloudy, the liquid feeding speed was increased to 12 g / min for phase inversion, and dropping was stopped when the liquid feeding amount reached 1050 parts by mass. Thereafter, the solvent was removed under reduced pressure to obtain an aqueous dispersion [X] of amorphous polyester resin fine particles [X].

[Developer Production Examples 1 to 14]
To each of the toners [1] to [14], a ferrite carrier having a volume-based median diameter of 60 μm coated with a silicone resin is added so that the toner concentration becomes 6% by mass, and mixed by a V-type mixer. Thus, developers [1] to [14] were produced.

(1) Evaluation of low-temperature fixability In a commercially available copier “bizhub PRO C6550” (manufactured by Konica Minolta Business Technologies) as an image forming apparatus, the surface temperature of the fixing heating roller in the fixing means of the heat roller fixing method is set to 120 to A developer modified so that it can be changed to a range of 200 ° C. is used. Developers [1] to [14] are mounted as developers, respectively, and in a normal temperature and normal humidity (temperature 20 ° C., humidity 50% RH) environment, A4 A fixing experiment for fixing a solid image having a toner adhesion amount of 8 mg / cm @ 2 on high-quality paper of a size was repeated up to 200.degree. C. while changing the fixing temperature to be increased from 120.degree. C. in increments of 5.degree. Of fixing experiments in which image stain due to low temperature offset was not visually observed, the lowest temperature was evaluated as the lowest fixing temperature. A sample having a minimum fixing temperature of 140 ° C. or lower was judged acceptable. The results are shown in Table 5.

(2) Long-term stability of charging performance A commercially available copying machine “bizhub PRO C6505” (manufactured by Konica Minolta Business Technologies) is used as an image forming apparatus, and developers [1] to [14] are mounted as developers. In a high-temperature and high-humidity environment (temperature of 30 ° C. and humidity of 85% RH), after continuously printing 100,000 character images with a printing rate of 10% on high-quality A4 size paper, white and halftone images were printed. A test image including the image was printed, fog was observed and image roughness of the halftone image was observed, and evaluation was performed according to the following evaluation criteria. The results are shown in Table 5.
-Evaluation criteria-
A: No decrease in image density or fog is observed visually. O: A decrease in image density and / or fog is observed with a magnifier of 20 times, but there is no practical problem. Δ: Decrease in image density and // Fog is visually observed, but there is no problem in practical use ×: Level in which image density reduction and fog are visually observed, and practically problematic

(3) Heat-resistant storage property For toners [1] to [14], 0.5 g of toner is placed in a 10 ml glass bottle with an inner diameter of 21 mm, the lid is closed, and a shaker “Tap Denser KYT-2000” (manufactured by Seishin Enterprise Co., Ltd.) is used. The mixture was shaken 600 times at room temperature, and then left for 2 hours in an environment with a temperature of 55 ° C. and a humidity of 35% RH with the lid open. Next, the toner is placed on a 48 mesh (aperture 350 μm) sieve, taking care not to break up the toner aggregates, and set in a “powder tester” (manufactured by Hosokawa Micron). Fix, adjust to vibration strength to give a feed width of 1 mm, apply vibration for 10 seconds, measure the ratio (mass%) of the amount of toner remaining on the sieve, and calculate the toner aggregation rate by the following formula (A) did. The heat resistant storage stability was evaluated based on the obtained toner aggregation rate. A toner having a toner aggregation rate of 20% or less was judged to be acceptable. The results are shown in Table 5.
Formula (A): toner aggregation rate (%) = (residual toner mass (g) on sieve) /0.5 (g) × 100

Claims (6)

An electrostatic charge image developing toner comprising toner particles containing a binder resin,
The binder resin has a domain matrix structure in which a crystalline polyester resin is dispersed as a domain phase in a matrix phase of an amorphous vinyl polymer formed using at least a vinyl monomer,
The amorphous vinyl polymer has a carboxy group concentration of 0.2 mmol / g or more and 1.0 mmol / g or less,
The toner for developing an electrostatic charge image, wherein the crystalline polyester resin has an ester group concentration of 0.1 mmol / g or more and 7.1 mmol / g or less.   The mass ratio of the amorphous vinyl polymer and the crystalline polyester resin (amorphous vinyl polymer / crystalline polyester resin) is 97/3 to 60/40. Toner for developing electrostatic images.   The toner for developing an electrostatic charge image according to claim 1, wherein the crystalline polyester resin has a melting point of 40 to 95 ° C. The amorphous vinyl polymer includes two types of amorphous vinyl polymer A and amorphous vinyl polymer B having different carboxy group concentrations,
The toner particles are obtained by agglomerating and fusing the composite fine particles in which the amorphous vinyl polymer B is adhered to the surfaces of the fine particles of the crystalline polyester resin and the fine particles of the amorphous vinyl polymer A. The electrostatic image developing toner according to any one of claims 1 to 3, wherein the toner is for developing an electrostatic image.   In the composite fine particles, a mass ratio of the crystalline polyester resin and the amorphous vinyl polymer B (crystalline polyester resin / amorphous vinyl polymer B) is 10/90 to 80/20. The toner for developing an electrostatic charge image according to claim 4. The amorphous vinyl polymer B in the composite fine particles has a carboxy group concentration of 0.2 mmol / g or more and 1.0 mmol / g or less,
When the carboxy group concentration of the amorphous vinyl polymer A is A1 [mmol / g] and the carboxy group concentration of the amorphous vinyl polymer B is B1 [mmol / g], the following relational expression (1) and The toner for developing an electrostatic charge image according to claim 4, wherein (2) is satisfied.
Relational expression (1): B1 <A1
Relational expression (2): A1-B1 ≦ | 0.5 |